US2016096142A1PendingUtilityA1
Method of making hollow fiber membrane modules with a curable composition and modules made therefrom
Est. expiryOct 1, 2034(~8.2 yrs left)· nominal 20-yr term from priority
Inventors:Joel M. HarrisDorian NelsonMichael S. MorenChristine M. GrieseAlbert M. GiorginiBrian W. Carlson
B01D 63/023B29L 2022/00B29C 65/002B01D 63/02
38
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Claims
Abstract
A method of making hollow fiber filtration modules including potting an end portion of a plurality of hollow fiber membranes with a multi-pack, solvent-free curable composition. The curable composition includes a Michael donor, a Michael acceptor, and a Michael reaction catalyst.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method of making a hollow fiber membrane module, comprising:
preparing a mixture of a multi-pack, solvent-free curable composition by combining a multi-functional Michael donor, a multi-functional Michael acceptor, and a Michael reaction catalyst, introducing the mixture of the curable composition into at least one end portion of a plurality of hollow fiber membranes, and allowing the curable composition to solidify and cure, thereby potting the end portion of the plurality of hollow fiber membranes.
2 . The method of claim 1 , wherein the curable composition further comprises from 0 to less than 10% by weight filler, based on the weight of the curable composition.
3 . The method of claim 1 , wherein the curable composition exhibits an initial viscosity of from 200 centipoise (cP) to 10,000 cP at 25° C.
4 . The method of claim 1 , wherein the multi-functional Michael donor comprises an acetoacetylated polyol that has at least one acetoacetoxy functional group, and a skeleton selected from the group consisting of a polyether polyol, a polyester polyol, a polycarbonate polyol, polyurethane polyol, urethane polyol, a polybutadiene polyol, a glycol, a mono-hydric alcohol, a polyhydric alcohol, a natural oil polyol, and modifications thereof, and combinations thereof.
5 . The method of claim 1 , wherein the multi-functional Michael acceptor is selected from the group consisting of monomers, oligomers, and polymers of multi-functional (meth)acrylate, and combinations thereof.
6 . The method of claim 5 , wherein the multi-functional Michael acceptor comprises multi-functional polyester acrylates, ethoxylated bisphenol A diacrylates, urethane acrylate oligomers, polyethylene glycol diacrylates, tricyclodecane dimethanol diacrylates, and combinations thereof.
7 . The method of claim 6 , wherein the curable composition exhibits, upon cure, non-foaming behavior in the presence of moisture.
8 . The method of claim 6 , wherein urethane acrylate oligomers comprises hexafunctional aromatic urethane acrylate oligomers, aliphatic polyester based urethane hexa-acrylate oligomers, and combinations thereof.
9 . The method of claim 1 , wherein the catalyst is a strong base catalyst having a conjugate acid that has a pKa of greater than 11.
10 . The method of claim 1 , wherein the catalyst comprises amindines and guanidines.
11 . The method of claim 9 , wherein the catalyst comprises 1,1,3,3-tetramethylguanidine (TMG), 1,8-diazabicyclo-[5.4.0]undes-7-ene (DBU), and 1,5-diazabicyclo[4,3,0]non-5-ene (DBN).
12 . The method of claim 1 , wherein the curable composition exhibits a maximum exotherm temperature of no greater than 120° C.
13 . The method of claim 1 , wherein the equivalent ratio of Michael acceptor functional group acrylates to Michael donor active hydrogens is from 0.3:1 to 1.5:1.
14 . The method of claim 1 , wherein the catalyst is in an amount of from 0.1% to 10% based on the mole of Michael active hydrogen atoms.
15 . The method of claim 1 , wherein the curable composition exhibits a gel time of from 3 minutes to 120 minutes.
16 . The method of claim 1 , wherein the curable composition exhibits a Shore A hardness of no less than 50 after cured for 7 days at 25° C. and 50% relative humidity.
17 . The method of claim 1 , wherein the curable composition exhibits a Shore D hardness of no less than 40 after cured for 7 days at 25° C. and 50% relative humidity.
18 . A hollow fiber membrane module, comprising
a plurality of hollow fiber membranes having at least one end portion potted with a potting composition,
wherein the potting composition comprises a reaction product of
a multi-functional Michael donor,
a multi-functional Michael acceptor, and
a Michael reaction catalyst.
19 . The hollow fiber membrane module of claim 18 , wherein the potting composition exhibits a Shore A hardness of no less than 50 after cured for 7 days at 25° C. and 50% relative humidity.
20 . The hollow fiber membrane module of claim 18 , wherein the potting composition exhibits non-foaming behavior in the presence of moisture.Cited by (0)
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